AzTrials
AzTrials

CancerRE-TREATNCT05126875

Re-TREAT: Re-irradiation for Relapsed Brain Metastases

A study testing Repeated stereotactic radiosurgery in people with Cancer and Brain Metastases, Adult, run by Copenhagen University Hospital, Rigshospitalet at 1 site in Denmark.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
Search all trials

Trial summary

The Re-TREAT study is a prospective clinical, phase 2, interventional, single-arm, multicenter trial for patients with local relapse of one or more brain metastases. Patients with recurrence of one or more brain metastases that have previously been treated with stereotactic radiosurgey (SRS) are treated with repeated… Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Cancer, Brain Metastases, Adult
What is being tested?
Repeated stereotactic radiosurgery
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
44 participants
Where
1 siteDenmark
Study dates
1 Jul 2021to 20 Aug 2023
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Brain metastases of solid tumor (carcinoma of unknown origin may be included but histological verification in case of BM alone is required)
  • Progression of previously treated lesion as decided by the multidisciplinary team conference
  • Previous single fraction SRS in area in question and dose plans must be available electronically
  • Previous single fraction SRS given > 3 months previously
  • ECOG (Eastern Cooperative Oncology Group) performance status ≤2
  • Life expectancy >3 months
  • Signed written consent.
  • Patients may have more than one recurring lesion and may also have new, untreated metastases which may be treated with standard SRS (up to a total of 4 metastases in accordance with Danish national guidelines).

Who cannot join

  • Two previous courses of radiotherapy for the same metastasis (e.g. SRS and WBRT)
  • Target lesions located in- or in proximity to eloquent brain areas that require reduction of radiotherapy dose
  • Target lesion gross tumor volume (GTV) for radiotherapy greater than 14,1 cm3 (equivalent to a sphere with a diameter of 3 cm)
  • Current or planned concomitant medical treatment that is likely to be active against brain metastases (e.g. tyrosine kinase inhibitors for EGFR-positive (epidermal growth factor receptor) non-small cell lung cancer) or that may influence interpretation of images (e.g. bevacizumab, a monoclonal antibody directed towards VEGF (vascular endothelial growth factor)) in the opinion of the investigators
  • Contraindication to magnetic resonance imaging using Gadolinium contrast enhancement (e.g. pacemaker, metallic implant or impaired renal function)
  • Rapid extracranial disease progression that in the opinion of the investigators confer a high risk of drop out from the study without evaluation scan at 3 months

Trial locations and contacts

1 site in 1 country.

Søren Møller, MD, PhD contact

+45 35451693

soeren.moeller.01@regionh.dk

Gitte F Persson, MD, PhD contact

+45 38689299

gitte.persson@regionh.dk

Denmark1 site, 1 recruiting
  • Rigshospitalet, University of Copenhagen

    Copenhagen, 2100

    Søren Møller, MD, +4535451693, soeren.moeller.01@regionh.dk

    Recruiting

Other trials in Denmark

About this study

Official title: Re-TREAT: A Phase 2 Study of Stereotactic Re-irradiation of Relapsed Brain Metastases

The Re-TREAT study is a prospective clinical, phase 2, interventional, single-arm, multicenter trial for patients with local relapse of one or more brain metastases. Patients with recurrence of one or more brain metastases that have previously been treated with stereotactic radiosurgey (SRS) are treated with repeated SRS. The aim is to evaluate the efficacy and toxicity of salvage SRS. The primary outcome is local control of the relapsed tumor and the secondary endpoints include toxicity as evaluated by the investigator and quality of life measured as a patient reported outcome. As an exploratory endpoint, the value of advanced MRI (magnetic resonance imaging) and PET (positron emission tomography) imaging as a biomarker for prediction of response to treatment or toxicity will be studied.

Read the detailed description

Background It is estimated that 10-20 % of patients with cancer develop brain metastases (BM) and the number is increasing due to prolonged patient survival as a result of improvements in surgery and systemic treatment. With few exceptions however, chemotherapy is not effective in treating disease within the central nervous system and therefore BM are often treated as a separate compartment independently from the rest of the disease throughout the body. Treatment modalities include surgical resection, stereotactic radiosurgery (SRS) and whole brain irradiation (WBI) or a combination.

SRS is a technique where a high dose of radiation is delivered through multiple fields, often as rotational intensity modulated radiation therapy (IMRT), where the beam is aimed at the tumor from everchanging angles, in order to minimize the dose to the surrounding tissue. In contrast to other radiation modalities, where a margin is added to the target in order to eradicate tumor cells that are not visible on imaging, SRS employs very small margins because brain metastases tend to be localized with sharp boundaries to surrounding tissue. The relative low dose absorbed by the surrounding tissue allows for delivery of the whole radiation dose to the tumor in one to three treatment sessions ('fractions'), as opposed to conventionally fractionated radiotherapy which is delivered in multiple fractions for the protection of surrounding healthy tissue.

As a whole, SRS results in high rates of local tumor control (65-90%) and low rates of toxicity (10-15%), which is usually mild. The most significant adverse event following SRS is radionecrosis, which is estimated to occur in 5-25% of patients. This is a condition which is poorly defined but is commonly used to describe a situation where the contrast enhancing area in the irradiated volume increases, often accompanied by increasing edema in the surrounding tissue. The condition may or may not cause symptoms. In cases of symptomatic, progressive radionecrosis, oral corticosteroids such as prednisolone may be needed for longer periods of time. Differentiation between relapsed metastasis and radionecrosis is notoriously difficult and represents one of the major diagnostic challenges in all of neuro-oncology. Advanced imaging techniques such as dynamic MRI (e.g. perfusion weighted images) or PET (positron emission tomography) have been used to aid in differentiation in experimental studies, but this currently remains an area of research. The development of the brain lesion over time and use of close follow-up using MRI will most often aid in interpretation of the images by the multidisciplinary team conference consisting of a radiologist, a radiation oncologist and a neurosurgeon.

There is no standard treatment in case of local tumor relapse following SRS. Patients who have not previously received WBI may be offered this, but the possible detrimental effects on neurocognition and quality of life are well documented4 and many clinicians as well as patients prefer to avoid this for as long as possible. Few patients in this category are recommended surgical resection.

Salvage SRS (repeated SRS to the same area at time of relapse) is commonly practiced at some institutions, Rigshospitalet being one of them, but the evidence to support routine use is sparse. The treatment has been evaluated only in retrospective studies. These have found high rates of local control (70-90%), but as adverse events and side effects cannot be evaluated from retrospective studies without risk of critical bias, the safety of this treatment remains to be established.

Aim of the study The Re-TREAT study is a prospective clinical, phase 2, interventional, single-arm, multicenter trial with patients with local relapse of one or more brain metastases. In the trial, they are treated with salvage SRS. The aim is to evaluate the efficacy and toxicity of salvage SRS. The primary outcome is local control of the relapsed tumor and the secondary endpoints include toxicity as evaluated by the investigator and quality of life measured as a patient reported outcome. As an exploratory endpoint, the value of advanced MRI and PET-imaging as a biomarker for prediction of response to treatment or toxicity will be studied.

Being tested
Repeated stereotactic radiosurgery
Medical subject headings
Neoplasms, Brain Neoplasms

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Repeated stereotactic radiosurgeryRadiation

    Also called SRS

    Repeated stereotactic radiosurgery to recurring brain metastases

Study groups in NCT05126875
Study groupRoleWhat they receive
Treatment armExperimentalTreatment with stereotactic radiosurgery
Receives: Radiation: Repeated stereotactic radiosurgery

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Freedom from progression of treated metastasis

    Freedom from progression of lesion size defined as stable or decreasing unidimensional measurement (longest diameter) on T1-weighted contrast enhanced magnetic resonance imaging (MRI)

    Measured: 3 months post treatment

Secondary outcomes (6)
  1. Adverse events

    Adverse events graded using National Cancer Institute (NCI) Common Toxicity Criteria (CTC) Adverse Events (AE) version 5.0

    Measured: 12 months

  2. Overall response

    Overall radiographic response of all treated lesions

    Measured: 3 months

  3. Neurological status

    Neurological status assessed by NANO (neurologic assessment in neuro-oncology) scale

    Measured: 6 months

  4. Time to intracranial relapse

    Time to recurrence of treated lesion or occurrence of new lesion(s)

    Measured: From date of treatment until the day of radiologically documented relapse in the brain assessed up to 12 months

  5. Overall survival

    Overall survival from entry into study

    Measured: From date of treatment until date of death from any cause assessed up to 12 months

  6. Patient reported outcomes

    Health related quality of life measured by the FACT-Br (Functional Assessment of Cancer Therapy - Brain) questionnaire

    Measured: 6 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted19 Nov 2021
  2. Study start1 Jul 2021
  3. Primary completion20 Aug 2023 (estimated)
  4. Study completion20 Aug 2023 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
44 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05126875
Sponsor's protocol ID
RE-TREAT
Acronym
RE-TREAT
Status last verified
Nov 2021
First submitted
9 Aug 2021
Last updated
19 Nov 2021
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Repeated stereotactic radiosurgery in people with Cancer and Brain Metastases, Adult, run by Copenhagen University Hospital, Rigshospitalet at 1 site in Denmark.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 8 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 19 Nov 2021. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Denmark. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Søren Møller, MD, PhD (+45 35451693, soeren.moeller.01@regionh.dk), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Freedom from progression of treated metastasis (time frame: 3 months post treatment). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 19 Nov 2021.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in